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Multiple nivolumab-induced CNS demyelination with spontaneous resolution in an asymptomatic metastatic melanoma patient

BACKGROUND: Immune checkpoint inhibitors (ICPis) have revolutionised the treatment of melanoma by significantly increasing survival rates and disease control. However, ICPis can have specific immune-related adverse events, including rare but severe neurological toxicity. CASE PRESENTATION: We report...

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Autores principales: Pillonel, Vincent, Dunet, Vincent, Hottinger, Andreas F., Berthod, Gregoire, Schiappacasse, Luis, Peters, Solange, Michielin, Olivier, Aedo-Lopez, Veronica
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6889661/
https://www.ncbi.nlm.nih.gov/pubmed/31791418
http://dx.doi.org/10.1186/s40425-019-0818-3
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author Pillonel, Vincent
Dunet, Vincent
Hottinger, Andreas F.
Berthod, Gregoire
Schiappacasse, Luis
Peters, Solange
Michielin, Olivier
Aedo-Lopez, Veronica
author_facet Pillonel, Vincent
Dunet, Vincent
Hottinger, Andreas F.
Berthod, Gregoire
Schiappacasse, Luis
Peters, Solange
Michielin, Olivier
Aedo-Lopez, Veronica
author_sort Pillonel, Vincent
collection PubMed
description BACKGROUND: Immune checkpoint inhibitors (ICPis) have revolutionised the treatment of melanoma by significantly increasing survival rates and disease control. However, ICPis can have specific immune-related adverse events, including rare but severe neurological toxicity. CASE PRESENTATION: We report a 44-year-old man diagnosed with stage IIIB melanoma who developed metastatic disease (pulmonary and brain metastases) and was treated with stereotactic radiosurgery and nivolumab immunotherapy. He developed asymptomatic multifocal diffuse white matter lesions consistent with active central nervous system demyelination seen on brain MRI. One month after cessation of the immunotherapy, spontaneous regression of the demyelinating lesions was observed, suggesting a nivolumab-related toxicity. CONCLUSION: We report the first case of a melanoma patient with an asymptomatic and spontaneously reversible central nervous system demyelination following nivolumab immunotherapy. This case highlights the need for better recognition of such atypical and rare neurological toxicities which could be mistaken for progressive brain metastases. Early recognition and appropriate management are crucial to reduce severity and duration of these toxicities, especially for patients with less favourable evolution.
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spelling pubmed-68896612019-12-11 Multiple nivolumab-induced CNS demyelination with spontaneous resolution in an asymptomatic metastatic melanoma patient Pillonel, Vincent Dunet, Vincent Hottinger, Andreas F. Berthod, Gregoire Schiappacasse, Luis Peters, Solange Michielin, Olivier Aedo-Lopez, Veronica J Immunother Cancer Case Report BACKGROUND: Immune checkpoint inhibitors (ICPis) have revolutionised the treatment of melanoma by significantly increasing survival rates and disease control. However, ICPis can have specific immune-related adverse events, including rare but severe neurological toxicity. CASE PRESENTATION: We report a 44-year-old man diagnosed with stage IIIB melanoma who developed metastatic disease (pulmonary and brain metastases) and was treated with stereotactic radiosurgery and nivolumab immunotherapy. He developed asymptomatic multifocal diffuse white matter lesions consistent with active central nervous system demyelination seen on brain MRI. One month after cessation of the immunotherapy, spontaneous regression of the demyelinating lesions was observed, suggesting a nivolumab-related toxicity. CONCLUSION: We report the first case of a melanoma patient with an asymptomatic and spontaneously reversible central nervous system demyelination following nivolumab immunotherapy. This case highlights the need for better recognition of such atypical and rare neurological toxicities which could be mistaken for progressive brain metastases. Early recognition and appropriate management are crucial to reduce severity and duration of these toxicities, especially for patients with less favourable evolution. BioMed Central 2019-12-02 /pmc/articles/PMC6889661/ /pubmed/31791418 http://dx.doi.org/10.1186/s40425-019-0818-3 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Case Report
Pillonel, Vincent
Dunet, Vincent
Hottinger, Andreas F.
Berthod, Gregoire
Schiappacasse, Luis
Peters, Solange
Michielin, Olivier
Aedo-Lopez, Veronica
Multiple nivolumab-induced CNS demyelination with spontaneous resolution in an asymptomatic metastatic melanoma patient
title Multiple nivolumab-induced CNS demyelination with spontaneous resolution in an asymptomatic metastatic melanoma patient
title_full Multiple nivolumab-induced CNS demyelination with spontaneous resolution in an asymptomatic metastatic melanoma patient
title_fullStr Multiple nivolumab-induced CNS demyelination with spontaneous resolution in an asymptomatic metastatic melanoma patient
title_full_unstemmed Multiple nivolumab-induced CNS demyelination with spontaneous resolution in an asymptomatic metastatic melanoma patient
title_short Multiple nivolumab-induced CNS demyelination with spontaneous resolution in an asymptomatic metastatic melanoma patient
title_sort multiple nivolumab-induced cns demyelination with spontaneous resolution in an asymptomatic metastatic melanoma patient
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6889661/
https://www.ncbi.nlm.nih.gov/pubmed/31791418
http://dx.doi.org/10.1186/s40425-019-0818-3
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